Clinical characteristics of primary pulmonary hemangiosarcoma outcomes: a Surveillance, Epidemiology, and End Results database analysis.

IF 1.6 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2025-08-15 eCollection Date: 2025-01-01 DOI:10.62347/VHRY6983
Jia-Chun Sun, Zi-Han Yang, Hao-Lin Shi, Ting-Ting Wei, Bo Sun, Jing-Xiang Su, Hong-Yan Liu, Qing-Feng Wang, Xin-Yang Li
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引用次数: 0

Abstract

Primary pulmonary hemangiosarcoma (PPHS) is an extraordinarily rare disorder. The objective of this study was to investigate the demographic characteristics and prognostic factors of patients with PPHS. Patients diagnosed with PPHS between 2000 and 2020 based on data from the Surveillance, Epidemiology, and End Results (SEER) database were retrospectively analyzed. Survival analysis was performed using the survival package of R (4.2.0). Univariate and multivariate Cox proportional hazards models were used to analyze independent prognostic factors. A nomogram was constructed by the R Regression Modeling Strategies (rms) package. A total of 123 patients with PPHS were included in this study; their mean survival time was 13.8 months. Further investigation revealed that the disease-specific survival rates of patients with PPHS at 1, 2, 3, and 5 years were 20.17%, 14.29%, 10.08%, and 5.88% respectively. In the regression analysis, age, tumor status, and treatment were identified as risk factors for patients with PPHS. In addition, chemotherapy was crucial for the treatment of patients with PPHS (P < 0.05). Finally, the nomogram we constructed to predict 0.5-, 1-, 2-, and 3-year disease-specific survival in patients with PPHS showed good accuracy (concordance index: 0.769). Age, tumor laterality, and tumor size were independent factors affecting the prognosis of patients with PPHS, and chemotherapy may significantly improve the long-term prognosis.

原发性肺血管肉瘤的临床特点:监测、流行病学和最终结果数据库分析。
原发性肺血管肉瘤(PPHS)是一种非常罕见的疾病。本研究的目的是探讨PPHS患者的人口学特征和预后因素。根据监测、流行病学和最终结果(SEER)数据库的数据,回顾性分析2000年至2020年间诊断为PPHS的患者。采用R(4.2.0)生存包进行生存分析。采用单因素和多因素Cox比例风险模型分析独立预后因素。利用R回归建模策略(rms)包构建了nomogram。本研究共纳入123例PPHS患者;平均生存时间为13.8个月。进一步调查发现,PPHS患者1、2、3、5年的疾病特异性生存率分别为20.17%、14.29%、10.08%、5.88%。在回归分析中,年龄、肿瘤状态和治疗被确定为PPHS患者的危险因素。化疗对PPHS患者的治疗至关重要(P < 0.05)。最后,我们构建的预测PPHS患者0.5年、1年、2年和3年疾病特异性生存的nomogram显示出良好的准确性(一致性指数:0.769)。年龄、肿瘤侧边、肿瘤大小是影响PPHS患者预后的独立因素,化疗可显著改善PPHS患者的远期预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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552
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